Disease #00957 (JBTS2 (Joubert syndrome, type 2), OMIM:608091)
Official abbreviation |
JBTS2 |
Name |
Joubert syndrome, type 2 |
OMIM ID |
608091 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
26 |
Phenotype entries for this disease |
20 |
Associated with 1 gene |
TMEM216 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2024-09-09 19:40:44 +02:00 (CEST) |
Individuals
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